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Macular ganglion cell-inner plexiform layer defect patterns in multiple sclerosis patients without optic neuritis: A
Valeria Albano1, Rosanna Dammacco1, Alessia Manni2
1Department of Neurosciences, Institute of Ophthalmology, University of Bari, Bari, Italy.
Multiple sclerosis patients without optic neuritis history show frequent macular ganglion cell-inner plexiform layer complex defects, primarily of the inner type. This finding may indicate subclinical optic nerve damage in MS.
Area of Science:
- Ophthalmology
- Neurology
- Medical Imaging
Background:
- Multiple sclerosis (MS) is a demyelinating disease affecting the central nervous system.
- Subclinical optic nerve involvement is common in MS, even without a history of optic neuritis.
- Spectral-domain optical coherence tomography (SD-OCT) is a key imaging technique for evaluating retinal nerve fiber layer and macular structures.
Purpose of the Study:
- To investigate the proportion and types of macular ganglion cell-inner plexiform layer complex (mGCIP) defects in patients with multiple sclerosis without a history of optic neuritis (MSNON).
- To compare mGCIP defect patterns between MSNON patients and healthy controls (HCs).
Main Methods:
- A cross-sectional, case-control study involving 17 MSNON patients and 17 HCs.
- SD-OCT (Zeiss Cirrus HD-OCT 4000) was used for mGCIP thickness measurement.
- mGCIP defect patterns were classified into nine types based on deviation map analysis.
Main Results:
- A mGCIP defect pattern was identified in 70.5% of MSNON eyes.
- The most prevalent defect pattern was the inner type (47%), followed by outer and inferior confined types (11.7% each).
- No mGCIP defects were observed in healthy controls.
Conclusions:
- MSNON patients exhibit significant mGCIP thinning, frequently characterized by inner defects.
- These mGCIP defects may serve as a valuable biomarker for detecting subclinical optic nerve involvement in MS.
- SD-OCT analysis of mGCIP patterns offers insights into early neurodegeneration in MS.
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